Protein decoy assembly using short fragments under geometric constraints

被引:29
作者
Kolodny, R
Levitt, M
机构
[1] Stanford Univ, Dept Biol Struct, Stanford, CA 94305 USA
[2] Stanford Univ, Dept Comp Sci, Stanford, CA 94305 USA
关键词
protein decoy assembly; discrete comformation space; geometric constraints; CONSISTENT FORCE-FIELD; STRUCTURE PREDICTION; CONFORMATIONS; ENTHALPIES; MODEL;
D O I
10.1002/bip.10262
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
A small set of protein fragments can represent adequately all known local protein structure. This set of fragments, along with a construction scheme that assembles these fragments into structures, defines a discrete (relatively small) conformation space, which approximates protein structures accurately. We generate protein decoys by sampling geometrically valid structures from this conformation space, biased by the secondary structure prediction for the protein. Unlike other methods, secondary structure prediction is the only protein-specific information used for generating the decoys. Nevertheless, these decoys are qualitatively similar to those found by others. The method works well for all-alpha proteins, and shows promising results for alpha and beta proteins. (C) 2003 Wiley Periodicals, Inc.
引用
收藏
页码:278 / 285
页数:8
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